Results 141 to 150 of about 4,054 (202)

Dentinogenesis imperfecta type II: a case report

open access: gold, 2021
Bruno Carvalho Albeny Morais   +4 more
openalex   +2 more sources

Study of enamel and dentin in primary teeth with dentinogenesis imperfecta type I: A case report [PDF]

open access: gold, 2019
Yoko Kamasaki   +4 more
openalex   +1 more source

Dentin Sialophosphoprotein Knockout Mouse Teeth Display Widened Predentin Zone and Develop Defective Dentin Mineralization Similar to Human Dentinogenesis Imperfecta Type III [PDF]

open access: hybrid, 2003
Taduru Sreenath   +9 more
openalex   +3 more sources

Dentinogenesis imperfecta type II: approach for dental treatment

open access: yesRevista de Odontologia da UNESP
INTRODUCTION: Dentinogenesis imperfecta (DI) is a hereditary dentin development disorder that affects both primary and permanent dentitions. The DI characteristics are discolored and translucent teeth ranging from gray to brownish-blue or amber.
Raquel Mantuaneli Scarel-Caminaga   +5 more
doaj  

Dentinogenesis imperfecta type II in Swedish children and adolescents. [PDF]

open access: yesOrphanet J Rare Dis, 2018
Andersson K   +3 more
europepmc   +1 more source

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